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Oral mucositis & oral health related quality of life in women undergoing chemotherapy for breast cancer in Karachi, Pakistan: A multicenter hospital based cross-sectional study

PloS one, 2024-04, Vol.19 (4), p.e0295456-e0295456

2024

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Association Between Ki-67 Proliferative Index and Oncotype-Dx Recurrence Score in Hormone Receptor-Positive, HER2-Negative Early Breast Cancers. A Systematic Review of the Literature

Breast cancer : basic and clinical research, 2024-01, Vol.18, p.11782234241255211-11782234241255211

2024

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Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

American journal of human genetics, 2009-11, Vol.85 (5), p.699-705

2009

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Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta

American journal of human genetics, 2013-02, Vol.92 (2), p.307-312

2013

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Decision making on antenatal screening results: A comparative Q‐method study of women from two Chinese cities

Health expectations : an international journal of public participation in health care and health policy, 2021-04, Vol.24 (2), p.363-376

2021

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A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

Nature genetics, 2005-04, Vol.37 (4), p.353-355

2005

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Exploring treatment outcomes in Stage II-III rectal cancer patients undergoing neoadjuvant therapy at a tertiary care center in Pakistan: a comprehensive analysis of pathological outcomes

BMC cancer, 2024-04, Vol.24 (1), p.479-479, Article 479

2024

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INFLUENCE OF CANCER NEWS ON QUALITY OF LIFE OF PATIENT'S FAMILIES: AN OBSERVATIONAL STUDY

Hematology, Transfusion and Cell Therapy, 2022-10, Vol.44, p.S26

2022

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EFFICACY OF FUROSEMIDE IN METHOTREXATE CLEARANCE IN PATIENTS TREATED WITH HIGH DOSE METHOTREXATE

Hematology, Transfusion and Cell Therapy, 2022-10, Vol.44, p.S34

2022

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Genetic and Epigenetic Analysis of Recurrent Hydatidiform Mole

Human mutation, 2009-05, Vol.30 (5), p.E629-E639

2009

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Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan

Hereditary cancer in clinical practice, 2022-06, Vol.20 (1), p.1-24, Article 24

2022

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Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation

American journal of human genetics, 2004-08, Vol.75 (2), p.261-266

2004

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Trick or Treat: Curative Management of Esophageal Squamous Cell Carcinoma of a COVID-positive Patient

Advances in Bioscience and Clinical Medicine, 2022-10, Vol.10 (4), p.9-12

2022

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Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain

American journal of human genetics, 2002-07, Vol.71 (1), p.136-142

2002

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Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice

American journal of human genetics, 2009-05, Vol.84 (5), p.683-691

2009

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Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size

American journal of human genetics, 2003-11, Vol.73 (5), p.1170-1177

2003

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Mean level of pretreatment neutrophil to lymphocyte ratio in patients with squamous cell carcinoma of the head and neck–Cross-sectional study

Heliyon, 2023-05, Vol.9 (5), p.e15894-e15894, Article e15894

2023

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Cascade screening for beta-thalassemia in Pakistan: development, feasibility and acceptability of a decision support intervention for relatives

European journal of human genetics : EJHG, 2022-01, Vol.30 (1), p.73-80

2022

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Healthcare professionals' perceptions of implementing a decision support intervention for cascade screening for beta-thalassemia in Pakistan

European journal of human genetics : EJHG, 2022-07, Vol.30 (7), p.795-799

2022

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Cascade screening for beta-thalassaemia in Pakistan: relatives' experiences of a decision support intervention in routine practice

European journal of human genetics : EJHG, 2022-04, Vol.30 (4), p.406-412

2022

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A Fifth Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 1q31

American journal of human genetics, 2000-12, Vol.67 (6), p.1578-1580

2000

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Esophageal squamous cell carcinoma in a patient with BRCA1 mutation: a rare association

Ecancermedicalscience, 2024-07, Vol.18

2024

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Role of circulating-tumor DNA in the early-stage non-small cell lung carcinoma as a predictive biomarker

Pathology, research and practice, 2023-05, Vol.245, p.154455-154455, Article 154455

2023

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Autonomous decision-making for antenatal screening in Pakistan: views held by women, men and health professionals in a low-middle income country

European journal of human genetics : EJHG, 2019-06, Vol.27 (6), p.848-856

2019

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Oral mucositis & oral health related quality of life in women undergoing chemotherapy for breast cancer in Karachi, Pakistan: A multicenter hospital based cross-sectional study

Association Between Ki-67 Proliferative Index and Oncotype-Dx Recurrence Score in Hormone Receptor-Positive, HER2-Negative Early Breast Cancers. A Systematic Review of the Literature

Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta

Decision making on antenatal screening results: A comparative Q‐method study of women from two Chinese cities

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

Exploring treatment outcomes in Stage II-III rectal cancer patients undergoing neoadjuvant therapy at a tertiary care center in Pakistan: a comprehensive analysis of pathological outcomes

INFLUENCE OF CANCER NEWS ON QUALITY OF LIFE OF PATIENT'S FAMILIES: AN OBSERVATIONAL STUDY

EFFICACY OF FUROSEMIDE IN METHOTREXATE CLEARANCE IN PATIENTS TREATED WITH HIGH DOSE METHOTREXATE

Genetic and Epigenetic Analysis of Recurrent Hydatidiform Mole

Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan

Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation

Trick or Treat: Curative Management of Esophageal Squamous Cell Carcinoma of a COVID-positive Patient

Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain

Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice

Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size

Mean level of pretreatment neutrophil to lymphocyte ratio in patients with squamous cell carcinoma of the head and neck–Cross-sectional study

Cascade screening for beta-thalassemia in Pakistan: development, feasibility and acceptability of a decision support intervention for relatives

Healthcare professionals' perceptions of implementing a decision support intervention for cascade screening for beta-thalassemia in Pakistan

Cascade screening for beta-thalassaemia in Pakistan: relatives' experiences of a decision support intervention in routine practice

A Fifth Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 1q31

Esophageal squamous cell carcinoma in a patient with BRCA1 mutation: a rare association

Role of circulating-tumor DNA in the early-stage non-small cell lung carcinoma as a predictive biomarker

Autonomous decision-making for antenatal screening in Pakistan: views held by women, men and health professionals in a low-middle income country

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